# hereditary spastic paraplegia 55

> gene (12q24.31) encoding probable peptide chain release factor C12orf65, mitochondrial.

**Wikidata**: [Q32143192](https://www.wikidata.org/wiki/Q32143192)  
**Source**: https://4ort.xyz/entity/hereditary-spastic-paraplegia-55


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55).
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)